A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233038



Internal ID20800078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139028244..139033080hg38UCSC Ensembl
chr7:138712990..138717826hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg384837
hg194837
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415821
Supporting Variants
Samples
Known GenesZC3HAV1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233038
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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